FDA 510(k), K133566, ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM WITH THE PERIPHERAL ROTALINK PLUS

FDA 510(k), K133566, ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM WITH THE PERIPHERAL ROTALINK PLUS

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510(K) Number: K133566
Device Name: ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM WITH THE PERIPHERAL ROTALINK PLUS
Manufacturer: BOSTON SCIENTIFIC CORP.
Device Classification Name: catheter, peripheral, atherectomy
Regulation Number: 870.4875
Classification Product Code: MCW
Date Received: 11/20/2013
Decision Date: 12/20/2013
Regulation Medical Specialty: Cardiovascular

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